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Mcad Deficiency
MCAD deficiency
Overview
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Related in the Kosmos
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Inborn errors of metabolism
(106)
Argininosuccinic acidemia
Beta-ketothiolase deficiency
Carnitine uptake defect
Citrullinemia
Galactosemia
Galactosemia
Glutaric acidemia type 2
Glutaric acidemia type I
HMG-CoA lyase deficiency
Isovaleric acidemia
LCHAD
MSUD
Metabolic diseases
Methylcrotonyl-CoA carboxylase deficiency
Methylmalonic acidemia
Newborn screening
PKU
Propionic acidemia
SCAD deficiency
Trifunctional protein deficiency
VLCAD
2,4 Dienoyl-CoA reductase deficiency
2-Methylbutyryl-CoA dehydrogenase deficiency
3-hydroxya- cyl-coenzyme A dehydrogenase deficiency
Acatalasia
Acid lipase disease
Adenosine deaminase deficiency
Adenylosuccinate lyase deficiency
Aldolase A deficiency
Analbuminaemia
Arakawa's syndrome II
Argininemia
Aspartylgl- ucosaminuria
Carbamoyl phosphate synthetase I deficiency
Carnitine palmitoylt- ransferase I deficiency
Carnitine palmitoylt- ransferase II deficiency
Carnitine-- acylcarnitine translocase deficiency
Cholesteryl ester storage disease
Congenital disorder of glycosylation
Crigler-Najjar syndrome
D-Glyceric acidemia
DOOR syndrome
Dihydropyrimidine dehydrogenase deficiency
Disaccharidase
Essential fructosuria
Fucosidosis
Fumarase deficiency
Galactose-- 1-phosphate uridylyltransferase galactosemia
Glucose-galactose malabsorption
Glycogen storage disease
Glycogen storage disease type I
Glycogen storage disease type II
Glycogen storage disease type III
Glycogen storage disease type V
Guanidinoacetate methyltransferase deficiency
Hawkinsinuria
Hereditary fructose intolerance
Histidinemia
Holocarboxylase synthetase deficiency
Hyperlysinemia
Hypermethioninemia
Hyperprolinemia
Hypervalinemia
Idiosyncrasy
Inborn error of lipid metabolism
Isobutyryl-coenzyme A dehydrogenase deficiency
Krabbe disease
Lecithin cholesterol acyltransferase deficiency
Lesch–Nyhan syndrome
Lipid storage disorder
Lipid storage disorders
Lysinuric protein intolerance
Lysosomal storage disease
Lysosomal storage diseases
Malonyl-CoA decarboxylase deficiency
Menkes disease
Metab-L
Methylmalonyl-CoA mutase deficiency
Mevalonate kinase deficiency
Myoadenylate deaminase deficiency
N-Acetylglutamate synthase deficiency
Niemann-Pick disease, type C
Organic acidemia
Ornithine transcarbamylase deficiency
Ornithine translocase deficiency
Prolidase deficiency
Pyruvate carboxylase deficiency
Pyruvate kinase deficiency
Refsum's disease
Rotor syndrome
Sarcosinemia
Schindler disease
Sly syndrome
Smith-Lemli-Opitz syndrome
Succinic semialdehyde dehydrogenase deficiency
Tangier disease
Tetrahydrobiopterin deficiency
Trimethylaminuria
Type I tyrosinemia
Type III tyrosinemia
Tyrosinemia
Tyrosinemia type II
Urea cycle disorder
Urocanic aciduria
Wolman disease
X-linked ichthyosis
Zellweger syndrome
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Autosomal recessive disorders
(21)
Biotinidase deficiency
Homocystinuria
Hb S
Congenital adrenal hyperplasia
Cystic fibrosis
Cystic fibrosis
Glutaric acidemia type I
VLCAD
Trifunctional protein deficiency
Carnitine uptake defect
SCAD deficiency
LCHAD
Methylcrotonyl-CoA carboxylase deficiency
Beta-ketothiolase deficiency
PKU
Argininosuccinic acidemia
Isovaleric acidemia
Methylmalonic acidemia
Glutaric acidemia type 2
Citrullinemia
Propionic acidemia
MSUD
more...
Genetic disorders
(24)
Genetic disorder
Glutaric acidemia type I
VLCAD
Trifunctional protein deficiency
Carnitine uptake defect
Carnitine uptake defect
SCAD deficiency
LCHAD
Methylcrotonyl-CoA carboxylase deficiency
Beta-ketothiolase deficiency
PKU
Argininosuccinic acidemia
Isovaleric acidemia
Methylmalonic acidemia
HMG-CoA lyase deficiency
Glutaric acidemia type 2
Citrullinemia
Propionic acidemia
Biotinidase deficiency
MSUD
Galactosemia
Homocystinuria
Hb S
Congenital adrenal hyperplasia
Cystic fibrosis
more...
Metabolic disorders
Hypoglycemia
Inborn errors of metabolism
Galactosemia
Homocystinuria
Pediatrics
Congenital hypothyroidism
Reye syndrome
Inborn errors of metabolism
Newborn screening
Congenital adrenal hyperplasia
Metabolic diseases
Cystic fibrosis
Genetics
ACADM
Hereditary
Genetic disorder
Diseases and disorders
(23)
Fatty acid oxidation disorders
Fatty acid oxidation disorder
Atelosteogenesis type 2
Iodine deficiency
Trifunctional protein deficiency
Trifunctional protein deficiency
Carnitine uptake defect
Metabolic disorders
Beta-ketothiolase deficiency
PKU
Argininosuccinic acidemia
Methylmalonic acidemia
Citrullinemia
Biotinidase deficiency
MSUD
Galactosemia
Homocystinuria
Hb S
Hypoglycemia
Congenital hypothyroidism
Reye syndrome
Congenital adrenal hyperplasia
Metabolic diseases
Cystic fibrosis
more...
See also
(11)
Acyl CoA dehydrogenase
L-3-hydroxyacyl CoA dehydrogenase
Long-chain-acyl-CoA dehydrogenase
Mitochondrial trifunctional protein
Microsoft Certified Professional
Microsoft Certified Professional
Beta oxidation
Fatty acids
Carnitine
Tandem mass spectrometry
Hearing test
Biochemical genetics
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